Formation Of Carbocation Research Articles

Enhancing oil shale pyrolysis using metal-doped carbon quantum dot catalysts: A comprehensive behavioral, kinetic, and mechanistic analysis

Current oil shale extraction technologies face significant challenges, including high heating costs, slow pyrolysis reaction rates, and low efficiency, which hinder effective resource exploitation. To address these issues, this study synthesized three types of metal-doped carbon quantum dot (M/CQD) catalysts—Co/CQDs, Ni/CQDs, and Mn/CQDs—and tested their effects on the pyrolysis of oil shale. The introduction of these catalysts resulted in a notable enhancement of the pyrolysis process, reducing the required activation energy by approximately 40 % and lowering the initiation temperatures for Co/CQDs, Ni/CQDs, and Mn/CQDs by 64 °C, 62 °C, and 94 °C, respectively. Consequently, the yield of shale oil increased significantly by 23.1 %, 13.3 %, and 19.8 % for each catalyst. Kinetic and product analyses indicate that these catalysts facilitate electron transfer from organic molecules, promoting the formation of free radicals and the cleavage of C–C bonds. This enhancement leads to an increased production of short-chain hydrocarbons and a reduction in oxygenates and esters, thereby improving the quality of the shale oil. Further insights from Density Functional Theory (DFT) calculations suggest that the catalysts enhance pyrolysis by promoting the formation of carbocations and synergizing with radicals released from the shale, intensifying the pyrolysis process. This study not only elucidates the catalytic mechanisms that enhance oil shale pyrolysis but also offers a promising approach to overcome technological challenges in shale resource recovery, such as high heating costs and low efficiency, paving the way for more efficient and cleaner shale oil production.

Structural determination of a carbocation-derived rearrangement product observed during Thiele cage opening: insight into the mechanism of an alkyl-extended pinacol reaction

A substituted bishomocubane structure colloquially known as a Thiele cage was previously observed to undergo an alkyl-extended pinacol-type rearrangement, wherein 1,2-aryl migration and ketone formation occurred together with (or at least in close succession to) opening of a strained cyclobutane bond. While there was some indication that the rearrangement reaction might proceed via a stepwise process involving a sequence of carbocation intermediates, previous studies did not uncover any direct evidence for the formation of carbocations, and did not fully explain the regio- and stereospecificity of the reaction. Here we describe the isolation and detailed characterization of a second rearrangement product formed under the pinacol reaction conditions, the existence of which implicates the formation of discrete carbocation intermediates along the reaction pathway. Observation of this new product also finally explains the fate of any Thiele cage material that is converted to a carbocation, but which is not geometrically predisposed to react through a facile 1,2-aryl migration. As such, our findings resolve previous questions surrounding the origin of regio- and stereospecificity in the alkyl-extended pinacol rearrangement.

Synthesis of dihydrocarvone over dendritic ZSM-5 Zeolite: A comprehensive study of experimental, kinetics, and computational insights

This study explores the isomerization of limonene-1,2-epoxide (LE) from kinetic and mechanistic viewpoints, using a dendritic ZSM-5 zeolite (d-ZSM-5) as a highly selective catalyst for the formation of dihydrocarvone (DHC) in the form of diastereoisomers (cis + trans). Ethyl acetate, a green solvent, was used at mild reaction temperatures (50–––70 °C). DHC, which can also be extracted from caraway oil, is widely used as an intermediate for epoxylactone production and as a constituent in flavors and perfumes. Kinetic modeling of LE isomerization was performed using a reaction network with eight parallel reactions and the corresponding rate equations, derived from the assumption of the rate-limiting surface reactions. The large standard errors in the statistical results of some kinetic parameters of the initial data fitting suggested that three of those reactions can be neglected to describe the kinetic model more accurately. This refinement resulted in standard errors in the kinetic parameters lower than ca. 11 %, confirming the statistical reliability of the modified kinetic model. Activation energies of 41.1 and 162 kJ/mol were estimated for the formation of cis-DHC and trans-DHC, respectively. Density Functional Theory (DFT) calculations revealed the preferred pathway for both cis and trans-LE conversion to DHC and carveol. The rate-determining step, carbocation formation (ΔEact = 234 kJ/mol), precedes near-instantaneous dihydrocarvone formation under the studied conditions.

Promotion of lignin depolymerization and cellulose utilization via the coupling effects of DDQ pre-oxidation and HCOOH extraction

The full utilization of biomass plays an important role in the environment and energy. In this study, the coupling pretreatment of DDQ pre-oxidation and HCOOH extraction was employed to realize the separation and modification of three components of sugarcane bagasse for full utilization. Especially, the modified lignin was depolymerized to obtain aromatic monomers, and cellulose-rich residue was used to prepare lignocellulose straws. Furthermore, the coupling effects between DDQ pre-oxidation and HCOOH extraction on chemical and physical properties of modified lignin and lignocellulose straws were studied. In addition, the mechanism of lignin depolymerization and lignocellulose straw synthesis were explored as well as the mass balance of the biorefinery process. The results showed that the total yield of aromatic monomers increased by nearly 2 times and the conversion of lignin was 95.1 % after DDQ pre-oxidation. The mechanism showed that DDQ selectively oxidized Cα-OH bond of lignin to Cα = O bond, which not only avoided the formation of carbocation, but also reduced the bond dissociation energy of β-O-4 bond. Moreover, the tensile strength of hydrophobic lignocellulose straw increased by nearly 2 times and its flexural strength was 10.36 MPa. Modified lignin and modified cellulose were connected via hydrogen bonds, which enhanced the intermolecular crosslinking of molecules, thus improving the mechanical properties of lignocellulose straws. Besides, the maximum xylose relative content and concentration of xylose were 61.16 % and 17.57 g/L, respectively. This study provides a method for high-value and green utilization of sugarcane bagasse.

Acid‐Catalyzed Ring Opening Reaction of Cyclopropyl Carbinols with Acetonitrile to Synthesize Amides

AbstractA one‐pot protocol for the synthesis of amides has been developed by employing acetonitrile as nitrogen source and solvent. The reaction undergoes ring‐opening of cyclopropyl carbinols and in situ formation of homoallylic carbocation, which reacts with acetonitrile to give desired products. The substrate of this reaction is widely applicable and the desired products are obtained in moderate to good yields.

Stereoselective synthesis of gem-dihalopiperidines via the halo-aza-Prins cyclization reaction: access to piperidin-4-ones and pyridines.

An efficient methodology for the synthesis of 4,4-dihalopiperidine derivatives in excellent yields has been developed using N-(3-halobut-3-en-1-yl)-4-methylbenzenesulfonamide and an aldehyde catalyzed by In(OTf)3. The reaction involves an initial formation of a six-membered carbocation via the aza-Prins cyclization reaction followed by a nucleophilic attack by a halide ion to give 4,4-dihalopiperidine. The dihalopiperidine is converted to tetrahydropiperidinone using Ac2O/Et3N in DCM/H2O (1 : 1). It is also utilized for the synthesis of pyridine scaffolds by treatment with DBU. Furthermore, the dihalopiperidine is transformed to its enol ether derivatives using KOH in alcohol.

4-Hydroxybenzenesulfonic acid triggers rapid preparation of phenolic aerogel composites by ambient pressure drying

Phenolic aerogel composites, as an excellent thermal insulation material, have been used in aerospace to resist extreme working conditions of severe heating and intense mechanical stress. However, the high cost and lengthy preparation process seriously restricts their more extensive application. Herein, a novel strategy for rapid preparation of aerogel composites by ambient pressure drying is enabled by copolymerization with 4-hydroxybenzenesulfonic acid. That is, the reactive 4-hydroxybenzenesulfonic acid can serve as the acid catalyst to accelerate both the protonation step and the gelation step during the preparation process of phenolic aerogel. After copolymerization with 4-hydroxybenzenesulfonic acid, these sulfonic acid groups significantly accelerate the protonation of benzoxazine intermediates, leading to more carbocation formation. The activation energy of curing reaction is significant decreased from 300 kJ∙mol−1 to 90 kJ∙mol−1. Thus, 4-hydroxybenzenesulfonic acid containing phenol formaldehyde resin (PFS) aerogel precursors exhibit much faster gelation reaction (within 4 h) than phenol formaldehyde resin (PF) aerogel precursor (12 h), which further facilitates the preparation of phenolic aerogel composites with needled quartz fiber felt by ambient pressure drying. Importantly, the PFS aerogel composites exhibit excellent thermal insulation performance under low heat flux and good fire safety under high heat flux. Rapid gelation of PFS triggered by 4-hydroxybenzenesulfonic acid provides a new approach to develop phenolic aerogel composites with low energy consumption, low cost and short preparation cycle.

Solid state debromination of C60Br24 back to C60 with cesium iodide: kinetics, thermodynamics and mechanism

The bromofullerene C60Br24 undergoes a complete and quantitative debromination to C60 when it is mixed and ground in the solid state with cesium iodide (CsI). The kinetics of this unique solid state debromination reaction was studied with FT-IR spectroscopy on C60Br24 embedded in CsI pellet. The debromination rate constant was measured k = 8.4 x 10−4 s−1 and found independent from the C60Br24 concentration. Chemical thermodynamics calculations show that the C60Br24 debromination in CsI matrix is characterized by a largely favorable free energy of reaction (ΔGr) and the reaction is exothermal. A debromination mechanism is discussed in terms of concerted elimination of the bromide anions and formation of carbocations on the fullerene cage in agreement with the E1 type elimination reaction mechanism. The carbocations sites are reduced to radicals and stabilized as trivinylmethyl radicals (the reduction occurs by the action of iodide ions of CsI which are oxidized to molecular iodine) and then a rearrangement of the double bonds leads back to C60 quantitatively.

CALCULATION OF THERMODYNAMIC AND KINETIC PARAMETERS OF CATALYTIC CRACKING REACTIONS ON LEWIS AND BRØNSTED ACID SITES

Link for citation: Nazarova G.Y., Ivashkina E.N., Maltsev V.V. Calculation of thermodynamic and kinetic parameters of catalytic cracking reactions on Lewis and Brønsted acid sites. Bulletin of the Tomsk Polytechnic University. Geo Аssets Engineering, 2023, vol. 334, no. 7, рр. 214-225. In Rus. The relevance of the research is caused by the emerging necessity of developing a mathematical model to optimize the heterogeneous process of catalytic cracking. This tools should take into account both the chemical transformations of a wide range of hydrocarbon groups (different feedstock types), as well as the stages of adsorption, reactants diffusion, conversion of hydrocarbons on the catalyst surface, acid characteristics and pore size of the catalysts. The study of the hydrocarbon conversion patterns on Lewis or Brønsted acid sites using quantum-chemical modeling methods allow us to quantify the thermodynamic parameters of reactants adsorption, the kinetic parameters of carbocations formation and cracking on acid sites. These results are necessary to develop a mathematical model based on the of heterogeneous catalytic reaction mechanism. The aim of this work is to identify the level of quantum chemical theory and to determine the thermodynamic and kinetic parameters of reactants adsorption, carbenium ions formationand hydrocarbons cracking on Lewis and Brønsted acid sites. Methods: quantum-chemical modeling methods to optimize the molecular geometry of reactants and products of catalytic cracking reactions, calculate vibrational frequencies, thermodynamic parameters of adsorption and catalytic cracking of hydrocarbons and heteroatomic compounds with the participation of Bronsted and Lewis acid sites. Results. The chosen level of quantum-chemical theory allowed obtaining the results that are consistent with the laws of the process and the experimental reactivity of hydrocarbons in cracking reactions on acid catalysts. The thermodynamic parameters of the adsorption of C6–C16 hydrocarbons and thiophenes on Lewis and Brønsted acid sites were identified. We found that during the cracking of n-hexane on the Lewis acid site, the reaction is limited by the carbenium ion formation stage.The activation energy of this stage was 281,3 kJ/mol whereas the value for the cracking stage was 277,2 kJ/mol. Further study shows that the activation energy of carbenium ion formation from izohexane and C8–C10 alkanes with normal structure on the Lewis acid site was 257,6 and 279,2…277,9 kJ/mol. The most energetically favorable is the formation of carbocation from hexene at Brønsted acid sites (76,59 kJ/mol). The results of the work will be used to create a mathematical model of a heterogeneous process based on the Langmuir–Hinshelwood equations.

Regio- and Chemoselective Synthesis of 3-(Dihydrofuran-3(2H)-ylidene)isobenzofuran-1(3H)-imines via Tandem Alkynyl Prins- and Intramolecular Oxycyclization Reactions.

A metal-free Lewis acid-initiated protocol for the synthesis of highly substituted 3-(dihydrofuran-3(2H)-ylidene)isobenzofuran-1(3H)-imines from 2-(4-hydroxybut-1-yn-1-yl)benzamides and aldehydes has been demonstrated. The reaction involves the initial formation of dihydrofuranylidene carbocation via a Prins cyclization reaction using BF3·OEt2, followed by intramolecular cyclization to produce 3-(dihydrofuran-3(2H)-ylidene)isobenzofuran-1(3H)-imines up to E/Z = 6:1 with moderate to good yields. The methodology can also be used for the synthesis of 3-(dihydro-2H-pyran-3(4H)-ylidene)-isobenzofuran-1(3H)-imines. The strategy leads to the formation of two C-O bonds and one C-C bond with two different heterocycles connected by a tetra-substituted double bond. Post synthetic application of the reaction was extended for the synthesis of furanylidene isobenzofuranones in excellent yields.

Stereoselective Synthesis of Highly Functionalized Cyclohexenes via Strong-Acid-Mediated Endocyclic C-C Bond Cleavage of Monocyclopropanated Cyclopentadienes.

A stereoselective, solvent- and metal-free endocyclic C-C bond cleavage of monocyclopropanated cyclopentadienes mediated by strong acids was developed, leading to highly functionalized six-membered carbocycles with high stereocontrol. The critical step for this ring-expansion is the formation of a cyclopropyl carbocation that undergoes endocyclic ring opening via an SN2'-type attack of various nucleophiles. Subsequent synthetic transformations show the versatility of the resulting cyclohexenes for the synthesis of new compounds with nonconventional substitution patterns.

Catalytic Radical‐Polar Crossover Non‐Classical Semipinacol Rearrangements: The Sustainable Approach

Semipinacol rearrangement has brought several elegant methods for the rapid synthesis of various complex scaffolds and as a result, has been applied extensively in the total synthesis of natural products. Apart from the classical ways, where transition metal or acids catalyzes the formation of carbocation, the semipinacol rearrangement has seen numerous revolutions and now are being happening in an eco-friendly manner relying on a catalytic radical-polar crossover tool. These catalytic processes are mainly occurring through photocatalysis or electrocatalysis. This review will provide a brief idea of these developments.

Ultrafast C-C and C-N bond formation reactions in water microdroplets facilitated by the spontaneous generation of carbocations.

Carbocations are important electrophilic intermediates in organic chemistry, but their formation typically requires harsh conditions such as extremely low pH, elevated temperature, strong oxidants and/or expensive noble-metal catalysts. Herein, we report the spontaneous generation of highly reactive carbocations in water microdroplets by simply spraying a diarylmethanol aqueous solution. The formation of transient carbocations as well as their ultrafast in-droplet transformations through carbocation-involved C-C and C-N bond formation reactions are directly characterized by mass spectrometry. The intriguing formation and stabilization of carbocations are attributed to the super acidity of the positively charged water microdroplets as well as the high electric fields at the water-air interfaces. Without the utilization of external acids as catalysts, we believe that these microdroplet reactions would pose a new and sustainable way for the construction of aryl-substituted compounds.

Conjugative Stabilization versus Anchimeric Assistance in Carbocations.

In this study, an old concept of anchimeric assistance is viewed from a different angle. Primary cations with two different heteroatomic substituents in the α-position to the cationic carbon atom CHXY−CH2+ (X, Y = Me2N, MeO, Me3Si, Me2P, MeS, MeS, Br) can be stabilized by the migration of either the X or Y group to the cation center. In each case, the migration can be either complete, resulting in the transfer of the migrating group to the adjacent carbon atom and the formation of a secondary carbocation stabilized by the remaining heteroatom, or incomplete, leading to an anchimerically assisted iranium ion. For all combinations of the above groups, these transformations have been studied by theoretical analysis at the MP2/aug-cc-pVTZ level and were shown to occur depending on the ability of anchimeric assistance by X and Y, as well as the conformation of the starting primary carbocation. In the conformers of α-amino cations with the p-orbital, C−N bond and the nitrogen lone pair in one plane, the Me2N group migrates to the cationic center to give aziranium ions. Otherwise, the second heteroatom is shifted to give iminium ions, without or with very slight anchimeric assistance. In the α-methoxy cations, the MeO group can be shifted to the cationic center to give the O-anchimerically assisted ions as local minima, the global minima being the ions anchimerically assisted by another heteroatom. The electropositive silicon tends to migrate towards the cationic center, but with the formation of a π-complex of the Me3Si cation with the C=C bond rather than a Si-anchimerically assisted cation. The phosphorus atom can either fully migrate to the cationic center (X = P, Y = S, Se) or form anchimerically stabilized phosphiranium ions (X = P, Y = O, Si, Br). The order of the anchimeric assistance for the heaviest atoms decreases in the order Se >> S > Br.

Synthesis of α-(Trifluoromethyl)styrenes and 1,3-Di(trifluoromethyl)indanes via Electrophilic Activation of TMS Ethers of (Trifluoromethyl)benzyl Alcohols in Brønsted Acids.

TMS ethers of CF3-benzyl alcohols (and their heterocyclic analogues) undergo elimination of TMSOH molecule with the formation of α-(trifluoromethyl)styrenes in yields of up to 90% under the action of strong Brønsted acids TfOH or H2SO4. Under the acidic conditions upon prolongation of the reaction, the α-(trifluoromethyl)styrenes are further dimerized into cis-/trans-1,3-di(trifluoromethyl)indanes in yields of up to 100%. Plausible reaction mechanisms of these electrophilic transformations including the intermediate formation of CF3-benzyl carbocations are discussed.

Radical Redox Annulations: A General Light-Driven Method for the Synthesis of Saturated Heterocycles.

We introduce here a two-component annulation strategy that provides access to a diverse collection of five- and six-membered saturated heterocycles from aryl alkenes and a family of redox-active radical precursors bearing tethered nucleophiles. This transformation is mediated by a combination of an Ir(III) photocatalyst and a Brønsted acid under visible-light irradiation. A reductive proton-coupled electron transfer generates a reactive radical which undergoes addition to an alkene. Then, an oxidative radical-polar crossover step leading to carbocation formation is followed by ring closure through cyclization of the tethered nucleophile. A wide range of heterocycles are easily accessible, including pyrrolidines, piperidines, tetrahydrofurans, morpholines, δ-valerolactones, and dioxanones. We demonstrate the scope of this approach through broad structural variation of both reaction components. This method is amenable to gram-scale preparation and to complex fragment coupling.

A study on the production and engine analysis of organic liquid fuel from jatropha and castor oil by catalytic cracking over solid acid catalysts

Catalytic cracking of non-edible oils such as jatropha and castor was done in fixed bed catalytic reactor. The microporous catalysts such as Hβ, HY and HZSM-5 and mesoporous catalyst like AlMCM-41 were synthesised and characterised by XRD and BET surface area analyzer. The reaction parameters such as temperature of reaction, WHSV (Weight hourly space velocity) and reaction time were optimised over Hβ catalyst using jatropha oil. Organic liquid products (OLP) comprising of green gasoline (GG), green kerosene (GK) and green diesel (GD) and gaseous products were found to be major products. The liquid products were analysed using gas chromatograph (Shimadzu GC-9A) fitted with Apeizon-L packed column and gaseous products were analysed using Poropak Q column. The % conversion, yield of OLP and selectivity towards GG, GK and GD were found to be higher at temperature of 400 °C, WHSV of 4.8 h−1 and reaction time of 1 h. The cracking of jatropha oil was done over HY, HZSM-5 and AlMCM-41 at this optimised condition. Among the microporous materials HZSM-5 produced more OLP with more selectivity towards GG fraction (50%) but yielded higher % of gaseous products. While AlMCM-41 (Si/Al = 25) was selective towards middle distillates fraction like GK (45%) & GD (35%) and yielded low gaseous products. The mechanism of reaction proceeds via carbocation formation. The activity of HZSM-5 and AlMCM-41 were examined with castor oil. The OLP viability as a replacement fuel in a single-cylinder diesel engine under various loads was evaluated in an IC engine test. Here, we look at how different engine operating conditions affect fuel efficiency, Brake Thermal Efficiency (BTE), and emissions of Carbon Monoxide (CO), Carbon-di-oxide (CO2) and Nitrogen Oxide (NOx). Overall analysis indicates that OLP cracked from Jatropha oil serves as a best fuel in comparison with OLP obtained from Castor oil.

Decreased DNA Damage and Improved p53 Specificity of RITA Analogs.

Reactivation of p53 tumor-suppressor function by small molecules is an attractive strategy to defeat cancer. A potent p53-reactivating molecule RITA, which triggers p53-dependent apoptosis in human tumor cells in vitro and in vivo, exhibits p53-independent cytotoxicity due to modifications by detoxification enzyme Sulfotransferase 1A1 (SULT1A1), producing a reactive carbocation. Several synthetic modifications to RITA's heterocyclic scaffold lead to higher energy barriers for carbocation formation. In this study, we addressed the question whether RITA analogs NSC777196 and NSC782846 can induce p53-dependent apoptosis without SULT1A1-dependent DNA damage. We found that RITA analog NSC782846, but not NSC777196, induced p53-regulated genes, targeted oncogene addiction, and killed cancer cells upon p53 reactivation, but without induction of DNA damage and inhibition RNA pol II. Our results might demonstrate a method for designing more specific and potent RITA analogs to accelerate translation of p53-targeting compounds from laboratory bench to clinic.

Quantum Defects: What Pairs with the Aryl Group When Bonding to the sp2 Carbon Lattice of Single-Wall Carbon Nanotubes?

Aryl diazonium reactions are widely used to covalently modify graphitic electrodes and low-dimensional carbon materials, including the recent creation of organic color centers (OCCs) on single-wall carbon nanotube semiconductors. However, due to the experimental difficulties in resolving small functional groups over extensive carbon lattices, a basic question until now remains unanswered: what group, if any, is pairing with the aryl sp3 defect when breaking a C═C bond on the sp2 carbon lattice? Here, we show that water plays an unexpected role in completing the diazonium reaction with carbon nanotubes involving chlorosulfonic acid, acting as a nucleophilic agent that contributes -OH as the pairing group. By simply replacing water with other nucleophilic solvents, we find it is possible to create OCCs that feature an entirely new series of pairing groups, including -OCH3, -OC2H5, -OC3H7, -i-OC3H7, and -NH2, which allows us to systematically tailor the defect pairs and the optical properties of the resulting color centers. Enabled by these pairing groups, we further achieved the synthesis of OCCs with sterically bulky pairs that exhibit high purity defect photoluminescence effectively covering both the second near-infrared window and the telecom wavelengths. Our studies further suggest that these diazonium reactions proceed through the formation of carbocations in chlorosulfonic acid, rather than a radical mechanism that typically occurs in aqueous solutions. These findings uncover the unknown half of the sp3 defect pairs and provide a synthetic approach to control these defect color centers for quantum information, imaging, and sensing.

Ultrasound-assisted solid Lewis acid-catalyzed transesterification of Lesquerella fendleri oil for biodiesel synthesis

Biodiesel, a mixture of fatty acid methyl esters (FAME), is bio-renewable, non-toxic, biodegradable, and is an attractive alternative to petroleum diesel. This work studied the sonochemical transesterification of Lesquerella fendleri oil (LFO) using inexpensive solid Lewis acid (LA) catalysts with an aim to reduce environmental pollution and dependance on non-renewable fuel sources. Due to the presence of hydroxy fatty acid methyl esters (HFAME) in LFO (∼60%), in addition to producing biofuel it can also be used to generate chemically important estolides and cyclic lactones. AlCl3, SnCl2, and Sn(CH3COO)2 showed catalytic activity using direct immersion ultrasound (DI-US) among a list of LA catalysts investigated, with AlCl3 being the best catalyst. Ultrasound increased the reaction rate by facilitating carbocation formation of glyceridic carbons. Experiments were carried out at room temperature in a solvent range from 3:1 to 18:1 methanol-to-oil molar ratio and catalyst loading from 1 wt% to 6 wt% over 10 to 60 min sonication time at 48% ultrasound amplitude (roughly 17 W/cm2). Complete conversion (>99%) was achieved in 40 min with 5 wt% AlCl3 catalyst. A statistical regression analysis with STATA 14.0 software was performed to optimize process parameters. Chemical characterizations of the compounds were performed with nuclear magnetic resonance (NMR) spectroscopy (1H NMR &13C NMR), and % conversion of FAMEs was calculated from the 1H NMR spectra. The fatty acid profile was determined by GC-FID and GC–MS analysis. FT-IR spectroscopic analysis and thermogravimetric analysis (TGA) were performed to investigate the infrared absorption pattern of the compound and the volatility difference between Lesquerella fendleri biodiesel and oil under nitrogen atmosphere. Results indicate that this is a fast, green, energy-efficient, sustainable, and industrially applicable method for biodiesel production from LFO.